BEUDAMED
    FDA Adverse Event Injury Summary report: N

    EON

    MDR report key: 3182166 · Received June 14, 2013

    Report

    Report Number
    1627487-2013-06470
    Event Type
    Injury
    Date Received
    June 14, 2013
    Date of Event
    January 1, 2009
    Report Date
    May 20, 2013
    Manufacturer
    ST. JUDE MEDICAL - NEUROMODULATION
    Product Code
    LGW
    PMA / PMN Number
    P010032
    Adverse Event
    Yes
    Report Source
    Manufacturer report
    Reporter Location
    TX, US
    Reporter Occupation
    NOT APPLICABLE

    Narratives

    Additional Manufacturer Narrative · 1

    SJM HAS LIMITED INFO RELATED TO THE PT'S MEDICAL HISTORY AND IS UNABLE TO FORM AN OPINION AS TO THE RELEVANCY OF THE PT'S HISTORY TO THE EVENT REPORTED. SJM DEFERS TO THE PT'S PHYSICIAN REGARDING MEDICAL HISTORY.

    Description of Event or Problem · 1

    DEVICE 1 OF 3. REFERENCE MFR REPORTS: 1627487-2013-00471, 00472. IT WAS REPORTED THE PT HAD HER SCS SYSTEM REMOVED SOMETIME IN 2009 AND WAS IMPLANTED WITH A COMPETITOR'S SYSTEM. THE REASON FOR THE EXPLANT IS NOT KNOWN. NO FURTHER INFO IS AVAILABLE AT THIS TIME.

    Devices

    Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
    271607 EON SCS IPG LGW ST. JUDE MEDICAL - NEUROMODULATION 3716 47483

    Patients

    Seq Age Sex Outcome Treatment
    1 35 YR Other